Canonical Allele Identifier: CA1225114634

Gene: COQ8A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226965621G= , CM000663.2:g.226965621G=	GRCh38
NC_000001.10:g.227153322G= , CM000663.1:g.227153322G=	GRCh37
NC_000001.9:g.225219945G=	NCBI36
NG_012825.1:g.30385G=
NG_012825.2:g.73086G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000366777.4:c.589-50G= MANE Select	ENSP00000355739.3:n.589-50G=
ENST00000366779.6:c.*5316-50G=	ENSP00000355741.2:n.*5316-50G=
ENST00000676884.1:c.*5438-50G=	ENSP00000503200.1:n.*5438-50G=
ENST00000366777.3:c.589-50G=	ENSP00000355739.3:n.589-50G=
ENST00000366778.5:c.433-50G=	ENSP00000355740.1:n.433-50G=
ENST00000366779.5:c.589-50G=	ENSP00000355741.1:n.589-50G=
ENST00000478406.5:n.107-11828G=
ENST00000489044.1:n.800-50G=
NM_020247.4:c.589-50G=	NP_064632.2:n.589-50G=
XM_005273201.1:c.589-50G=	XP_005273258.1:n.589-50G=
XM_011544238.1:c.589-50G=	XP_011542540.1:n.589-50G=
XM_011544239.1:c.589-50G=	XP_011542541.1:n.589-50G=
XM_011544240.1:c.589-50G=	XP_011542542.1:n.589-50G=
XM_011544241.1:c.589-50G=	XP_011542543.1:n.589-50G=
XM_011544239.2:c.589-50G=	XP_011542541.1:n.589-50G=
XM_011544241.2:c.589-50G=	XP_011542543.1:n.589-50G=
XM_017001852.1:c.589-50G=	XP_016857341.1:n.589-50G=
XM_024448517.1:c.589-50G=	XP_024304285.1:n.589-50G=
XM_024448518.1:c.589-50G=	XP_024304286.1:n.589-50G=
NM_020247.5:c.589-50G= MANE Select	NP_064632.2:n.589-50G=